| (2'R*,5'R*,6'R*)-Form |
C₄₀H₅₈O₂ |
570.902 |
Momordica cochinchinensis |
Cucurbitaceae |
Yes |
|
Tetraterpenes |
http://terokit.qmclab.com/molecule.html?MolId=TKC046688 |
Maoka T, Yamano Y, Wada A, et al. Oxidative metabolites of lycopene and γ-carotene in gac (Momordica cochinchinensis). J Agric Food Chem. 2015;63(5):1622-1630. doi:10.1021/jf505008d |
| 1-(3,4-Dihydroxyphenyl)-1-Propanol |
C₂₁H₂₈O₆ |
376.449 |
Bupleurum fruticosum |
Umbelliferae |
Yes |
|
Hemiterpenes |
http://terokit.qmclab.com/molecule.html?MolId=TKC018623 |
-- |
| 16,24,25-Trihydroxycycloartane-3,6-dione |
C₃₀H₄₈O₅ |
488.709 |
Astragalus membranaceus |
Leguminosae |
Yes |
|
Triterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC047383 |
-- |
| 19(4)-Abeo-6,11-Epoxy-6,12-Dihydroxy-6,7-Seco-4(18),8,11,13-Abietatetraen-7-al |
C₂₀H₂₆O₄ |
330.424 |
Plectranthus barbatus |
Labiatae |
Yes |
|
Diterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC000002 |
Perrone A, Masullo M, Bassarello C, et al. Unusual cycloartane glycosides from Astragalus eremophilus[J]. Tetrahedron. 2008;64(22):5061-5071. doi:10.1016/j.tet.2008.03.069. |
| 1-Ketoaethiopinone |
C₂₀H₂₂O₃ |
310.393 |
Salvia argentea |
Labiatae |
Yes |
|
Diterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC000068 |
Michavila A, et al. 20-Nor-abietane and rearranged abietane diterpenoids from the root of Salvia argentea. 1986;25(8),1935–1937. doi:10.1016/s0031-9422(00)81178-4 |
| 2,4-Cyclo-11-Hydroxy-8-Eudesmanone |
C₁₅H₂₄O₂ |
236.355 |
Platycarya strobilacea |
Juglandaceae |
Yes |
|
Sesquiterpenes |
http://terokit.qmclab.com/molecule.html?MolId=TKC027804 |
-- |
| 2,4-Cyclo-7(11)-Eudesmen-8-one |
C₁₅H₂₂O |
218.34 |
Platycarya strobilacea |
Juglandaceae |
Yes |
|
Sesquiterpenes |
http://terokit.qmclab.com/molecule.html?MolId=TKC027809 |
-- |
| 2-C-methyl-D-erythritol 2,4-cyclic diphosphate |
C₅H₁₂O₉P₂ |
278.09 |
Arabidopsis thaliana |
Brassicaceae |
Yes |
|
Hemiterpenes |
http://terokit.qmclab.com/molecule.html?MolId=TKC018713 |
-- |
| 2-Hydroxy-2-Methylbutanoic Acid |
C₁₉H₂₆O₁₁ |
280.273 |
Rhodiola kirilowii |
Crassulaceae |
Yes |
|
Hemiterpenes |
http://terokit.qmclab.com/molecule.html?MolId=TKC018651 |
-- |
| 2-Hydroxy-2-Methylbutanoic Acid |
C₁₉H₂₆O₁₁ |
430.406 |
Clerodendrum bungei |
Verbenaceae |
Yes |
|
Hemiterpenes |
http://terokit.qmclab.com/molecule.html?MolId=TKC018652 |
-- |
| 2-Methyl-2-Butene-1,4-diol |
C₂₃H₃₂O₁₂ |
500.497 |
Eleutherococcus senticosus |
Araliaceae |
Yes |
|
Hemiterpenes |
http://terokit.qmclab.com/molecule.html?MolId=TKC018746 |
-- |
| 2-Methylbutyl Gentiobioside |
C₁₇H₃₂O₁₁ |
412.432 |
Solanum tuberosum |
Solanaceae |
Yes |
|
Hemiterpenes |
http://terokit.qmclab.com/molecule.html?MolId=TKC018734 |
-- |
| 3,11-Cyclo-1,2,5,9,10-Pentahydroxy-4(20)-Taxen-13-one |
C₃₃H₄₀O₉ |
580.674 |
Taxus baccata |
Taxaceae |
Yes |
|
Diterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC000102 |
Shi QW, Lederman Z, Sauriol F, McCollum RS, Zamir LO. A yew in Israel, new taxane derivatives. J Nat Prod. 2004;67(2):168-173. doi:10.1021/np030311y |
| 3,11-Cyclo-2,5,7,9,10-Pentahydroxy-4(20),5-Taxadien-13-one |
C₃₅H₄₀O₁₀ |
620.695 |
Taxus cuspidata |
Taxaceae |
Yes |
|
Diterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC000101 |
-- |
| 3,11-Cyclo-2,5,7,9,10-Pentahydroxy-4(20)-Taxen-13-one |
C₃₅H₄₂O₁₀ |
622.711 |
Taxus canadensis |
Taxaceae |
Yes |
|
Diterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC000103 |
Shi QW, Sauriol F, Mamer O, Zamir LO. New taxanes from the needles of Taxus canadensis. J Nat Prod. 2003;66(4):470-476. doi:10.1021/np020361n |
| 3,16,24,25-Tetrahydroxycycloartan-6-one |
C₃₀H₅₀O₅ |
490.725 |
Astragalus membranaceus |
Leguminosae |
Yes |
|
Triterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC047391 |
-- |
| 3,18-Cyclo-14-Oxo-8,13(15)-Abietadien-16,12-olide |
C₂₀H₂₄O₃ |
312.409 |
Euphorbia retusa |
Euphorbiaceae |
Yes |
|
Diterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC000100 |
-- |
| 3,18-Cyclo-7,17-Dihydroxy-8(14),13(15)-Abietadien-16,12-olide |
C₂₀H₂₆O₄ |
330.424 |
Suregada glomerulata |
Euphorbiaceae |
Yes |
|
Diterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC000030 |
Yan RY, Tan YX, Cui XQ, Chen RY, Yu DQ. Diterpenoids from the roots of Suregada glomerulata. J Nat Prod. 2008;71(2):195-198. doi:10.1021/np0705211 |
| 3',4',7-Trihydroxyflavanone |
C₃₇H₅₂O₁₂ |
688.811 |
Catharanthus roseus |
Apocynaceae |
Yes |
|
Sesquiterpenes |
http://terokit.qmclab.com/molecule.html?MolId=TKC026986 |
-- |
| 3,4-Dihydroxy-2-(Hydroxymethyl)Butanoic Acid |
C₁₁H₁₉NO₈ |
293.272 |
Rhodiola kirilowii |
Crassulaceae |
Yes |
|
Hemiterpenes |
http://terokit.qmclab.com/molecule.html?MolId=TKC018617 |
-- |
| 3',6'-Digalloylpaeoniflorin |
C₃₇H₃₆O₁₉ |
784.676 |
Paeonia obovata |
Paeoniaceae |
Yes |
|
Monoterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC018887 |
-- |
| 3,7-Dihydroxy-5,7-Megastigmadien-9-one |
C₁₉H₃₀O₈ |
386.441 |
Podocarpus elongatus |
Podocarpaceae |
Yes |
|
Sesquiterpenes |
http://terokit.qmclab.com/molecule.html?MolId=TKC023565 |
-- |
| 3-Hydroxymethyl-2(5H)-Furanone |
C₅H₆O₃ |
114.1 |
Hylotelephium telephium |
Crassulaceae |
Yes |
|
Hemiterpenes |
http://terokit.qmclab.com/molecule.html?MolId=TKC018689 |
Calderon A, De March P, Font J. Synthesis of 3-(1-hydroxyalkyl)furan-2(5H)-ones: unexpected substitution reaction in allylic alcohols by bromine[J]. ChemInform. 1988;19(11). doi:10.1002/chin.198811202. |
| 3-Methylbutanoic Acid |
C₅H₁₀O₂ |
102.133 |
Nicotiana tabacum |
Solanaceae |
Yes |
|
Hemiterpenes |
http://terokit.qmclab.com/molecule.html?MolId=TKC018731 |
Kaler G, Truong DM, Khandelwal A, et al. Structural variation governs substrate specificity for organic anion transporter (OAT) homologs. Potential remote sensing by OAT family members. J Biol Chem. 2007;282(33):23841-23853. doi:10.1074/jbc.M703467200 |
| 3-O-(3-Pyridinecarbonyl),8-O-(2,3-Dimethylbutanoyl),5,10,14,15-Tetra-Ac |
C₄₀H₅₁NO₁₄ |
769.841 |
Euphorbia seguieriana |
Euphorbiaceae |
Yes |
|
Diterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC000095 |
Jeske f, JakupovicJ. Berendsohn W. Diterpenes from euphorbia seguieriana. 1995;40(6),1743–1750. doi:10.1016/0031-9422(95)00514-8 |
| 4,7-Cyclo-3,15-Caryophyllanediol |
C₁₅H₂₆O₂ |
238.371 |
Ocimum tenuiflorum |
Labiatae |
Yes |
|
Sesquiterpenes |
http://terokit.qmclab.com/molecule.html?MolId=TKC027770 |
Singh D, Kumar CP, Darokar MP. New Antiproliferative Tricyclic Sesquiterpenoid from the Leaves of Ocimum sanctum. Helvetica Chimica Acta. 2014;97(5),708–711. doi:10.1002/hlca.201300269 |
| 4-Hydroxy-5-Methyl-3-Furancarboxylic Acid |
C₆H₆O₄ |
142.11 |
Capparis spinosa |
Capparaceae |
Yes |
|
Hemiterpenes |
http://terokit.qmclab.com/molecule.html?MolId=TKC018687 |
Yang T, Wang C, Liu H, Chou G, Cheng X, Wang Z. A new antioxidant compound from Capparis spinosa. Pharm Biol. 2010;48(5):589-594. doi:10.3109/13880200903214231 |
| 4-Hydroxysaprorthoquinone |
C₂₀H₂₆O₃ |
314.425 |
Salvia prionitis |
Labiatae |
Yes |
|
Diterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC000065 |
Lin LZ, Blaskó G, Cordell GA. Diterpenes of Salvia prionitis. 1989;28(1), 177–181. doi:10.1016/0031-9422(89)85033-2 |
| 4-O-Ethylpaeoniflorin |
C₂₅H₃₂O₁₁ |
508.52 |
Paeonia delavayi |
Paeoniaceae |
Yes |
|
Monoterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC018903 |
-- |
| 5,6-Epoxy-5,6-Dihydro-β,ε-Carotene-3,3'-diol |
C₄₀H₅₆O₃ |
584.885 |
Tussilago farfara |
Asteraceae |
Yes |
|
Tetraterpenes |
http://terokit.qmclab.com/molecule.html?MolId=TKC046785 |
-- |
| 5'-Acetoxy-8'-Hydroxyumbelliprenin |
C₂₆H₃₂O₆ |
440.536 |
Ferula assa-foetida |
Umbelliferae |
Yes |
|
Sesquiterpenes |
http://terokit.qmclab.com/molecule.html?MolId=TKC022712 |
-- |
| 6-Acetylajugol |
C₁₇H₂₆O₁₀ |
390.385 |
Betonica officinalis |
Labiatae |
Yes |
|
Monoterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC018942 |
Tasdemir D, Scapozza L, Zerbe O, Linden A, Calis I, Sticher O. Iridoid glycosides of Leonurus persicus. J Nat Prod. 1999;62(6):811-816. doi:10.1021/np980376e |
| 6'-Galloyllotaustralin |
C₁₈H₂₃NO₁₀ |
413.379 |
Euphorbia supina |
Euphorbiaceae |
Yes |
|
Hemiterpenes |
http://terokit.qmclab.com/molecule.html?MolId=TKC018649 |
-- |
| 6-O-(4-Hydroxy-3-Methoxybenzoyl)Ajugol |
C₂₃H₃₀O₁₂ |
498.481 |
Rehmannia glutinosa |
Orobanchaceae |
Yes |
|
Monoterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC018958 |
-- |
| 6-O-(4-Hydroxybenzoyl)Ajugol |
C₂₂H₂₈O₁₁ |
468.455 |
Rehmannia glutinosa |
Orobanchaceae |
Yes |
|
Monoterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC018956 |
-- |
| 6-O-P-Trans-Coumaroylajugol |
C₂₄H₃₀O₁₁ |
494.493 |
Rehmannia glutinosa |
Orobanchaceae |
Yes |
|
Monoterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC018957 |
-- |
| 6-O-Trans-Feruloylajugol |
C₂₅H₃₂O₁₂ |
524.519 |
Triaenophora rupestris |
Scrophulariaceae |
Yes |
|
Monoterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC018960 |
-- |
| 7,12-Cyclo-6,11-Epoxy-4-Dumortanol |
C₁₅H₂₄O₂ |
236.355 |
Dumortiera hirsuta |
Marchantiaceae |
Yes |
|
Sesquiterpenes |
http://terokit.qmclab.com/molecule.html?MolId=TKC027798 |
Alicia B, Kamiya N, Toyota M, et al. A 7-nordumortenone and other dumortane derivatives from the Argentine liverwort Dumortiera hirsuta[J]. Phytochemistry. 1999;51(2):281-287. doi:10.1016/S0031-9422(98)00772-9. |
| 7-Acetyl-12-Deacetyl-9-Deoxycyclobutatusin |
C₂₄H₃₂O₈ |
448.512 |
Plectranthus barbatus |
Labiatae |
Yes |
|
Diterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC000012 |
-- |
| 7-Hydroxy-1,6-Cyclo-2,10,14-Phytatrien-4-one |
C₂₀H₃₂O₂ |
304.474 |
Croton linearis |
Euphorbiaceae |
Yes |
|
Diterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC000111 |
Alexander IC, Pascoe KO, Manchard P, Williams LAD. An insecticidal diterpene from Croton linearis. 1991;30(6), 1801–1803. doi:10.1016/0031-9422(91)85016-s |
| 8(7)-Abeo-4,5-Epoxy-3-Hydroxy-7-Amorphanone |
C₁₅H₂₄O₃ |
252.354 |
Artemisia annua |
Asteraceae |
Yes |
|
Sesquiterpenes |
http://terokit.qmclab.com/molecule.html?MolId=TKC027755 |
Brown GD, Liang GY, Sy LK. Terpenoids from the seeds of Artemisia annua. Phytochemistry. 2003;64(1):303-323. doi:10.1016/s0031-9422(03)00294-2 |
| 8,14-Bis-O-(3-Pyridinecarbonyl),3-Propanoyl,5,10,15-Tri-Ac |
C₄₁H₄₆N₂O₁₄ |
790.819 |
Euphorbia seguieriana |
Euphorbiaceae |
Yes |
|
Diterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC000089 |
Jeske f, JakupovicJ. Berendsohn W. Diterpenes from euphorbia seguieriana. 1995;40(6),1743–1750. doi:10.1016/0031-9422(95)00514-8 |
| 8,15-Cyclo-15-Hydroxy-7,12-Labdadien-16-Oic Acid |
C₂₀H₃₀O₃ |
318.457 |
Curcuma kwangsiensis |
Zingiberaceae |
Yes |
|
Diterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC000071 |
-- |
| 8-Debenzoyl-8-Galloylpaeoniflorin |
C₂₃H₂₈O₁₄ |
528.463 |
Paeonia obovata |
Paeoniaceae |
Yes |
|
Monoterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC018929 |
-- |
| 8-Debenzoyl-8-Isovaleroylpaeoniflorin |
C₂₁H₃₂O₁₁ |
460.476 |
Paeonia obovata |
Paeoniaceae |
Yes |
|
Monoterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC018927 |
-- |
| 8-Debenzoylgalloylpaeoniflorin |
C₂₃H₂₈O₁₄ |
528.463 |
Paeonia obovata |
Paeoniaceae |
Yes |
|
Monoterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC018930 |
-- |
| Aduncin |
C₁₅H₁₈O₆ |
294.303 |
Dendrobium aduncum |
Orchidaceae |
Yes |
|
Sesquiterpenes |
http://terokit.qmclab.com/molecule.html?MolId=TKC027761 |
Gawell L, Leander K. The constitution of aduncin, a sesquiterpene related to picrotoxinin, found in Dendrobium aduncum[J]. Phytochemistry. 1976;15(12):1991–1992. doi:10.1016/S0031-9422(00)88869-X. |
| Aegyptinone A |
C₂₀H₂₂O₃ |
310.393 |
Salvia aegyptiaca |
Labiatae |
Yes |
|
Diterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC000006 |
Sabri NN, Abou-Donia AA, Ghazy NM, Assad AM, et al. Two new rearranged abietane diterpene quinones from Salvia aegyptiaca L. The Journal of Organic Chemistry. 1989;54(17),4097–4099. doi:10.1021/jo00278a021 |
| Agroastragaloside I |
C₄₅H₇₄O₁₆ |
871.071 |
Astragalus membranaceus |
Leguminosae |
Yes |
|
Triterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC047381 |
Hirotani M, Zhou Y, Rui H, Furuya T. Cycloartane triterpene glycosides from the hairy root cultures of Astragalus membranaceus. Phytochemistry. 1994;37(5):1403-1407. doi:10.1016/s0031-9422(00)90420-5 |
| Agroastragaloside II |
C₄₃H₇₂O₁₅ |
829.034 |
Astragalus membranaceus |
Leguminosae |
Yes |
|
Triterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC047377 |
Hirotani M, Zhou Y, Rui H, Furuya T. Cycloartane triterpene glycosides from the hairy root cultures of Astragalus membranaceus. Phytochemistry. 1994;37(5):1403-1407. doi:10.1016/s0031-9422(00)90420-5 |
| Ajugol |
C₁₅H₂₄O₉ |
348.348 |
Rehmannia glutinosa |
Orobanchaceae |
Yes |
|
Monoterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC018941 |
Xie CX, Zhang M, Li YJ, Geng XT, Wang FQ, Zhang CY. Comparison of chemical quality characteristics between radial striations and non-radial striations in tuberous root of Rehmannia glutinosa. China Journal of Chinese Materia Medica. 2017;42:21. doi:10.19540/j.cnki.cjcmm.20170905.004 |
| Alexandroside I |
C₃₆H₆₂O₁₀ |
654.882 |
Astragalus eremophilus |
Leguminosae |
No |
|
Triterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC047364 |
-- |
| Arjunolic Acid |
C₃₀H₄₈O₅ |
488.709 |
Ulmus pumila |
Ulmaceae |
Yes |
|
Triterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC022690 |
Gallo MB, Rocha WC, da Cunha US, et al. Bioactivity of extracts and isolated compounds from Vitex polygama (Verbenaceae) and Siphoneugena densiflora (Myrtaceae) against Spodoptera frugiperda (Lepidoptera: Noctuidae). Pest Manag Sci. 2006;62(11):1072-1081. doi:10.1002/ps.1278 |
| Artemisinin |
C₁₅H₂₂O₅ |
282.33 |
Artemisia annua |
Asteraceae |
Yes |
|
Sesquiterpenes |
http://medicinalplants.ynau.edu.cn/meta/bolites/532 |
-- |
| Askendoside A |
C₄₂H₇₀O₁₄ |
799.008 |
Astragalus eremophilus |
Leguminosae |
No |
|
Triterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC047354 |
Isaev MI, Gorovits MB, Abdullaev ND, Abubakirov NK. Triterpene glycosides ofAstragalusand their genins. XIV. Askendoside A fromAstragalus taschkendicus. 1983;19(5), 552–556. doi:10.1007/bf00576081 |
| Askendoside C |
C₄₀H₆₈O₁₃ |
756.971 |
Astragalus eremophilus |
Leguminosae |
No |
|
Triterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC047358 |
-- |
| Askendoside F |
C₄₆H₇₈O₁₈ |
919.112 |
Astragalus eremophilus |
Leguminosae |
No |
|
Triterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC047361 |
Isaev MI. Triterpene glycosides ofAstragalusand their genins. 1995;31(6),690–693. doi:10.1007/bf01386181 |
| Askendoside G |
C₄₇H₈₀O₁₈ |
933.139 |
Astragalus eremophilus |
Leguminosae |
No |
|
Triterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC047360 |
Isaev MI. Triterpene glycosides ofAstragalusand their genins. Liv. askendoside G fromAstragalus taschkendicus. 1996;32(5),706–709. doi:10.1007/bf01375119 |
| Asperuloside |
C₁₈H₂₂O₁₁ |
414.363 |
Arabidopsis thaliana |
Brassicaceae |
Yes |
|
Monoterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC018873 |
-- |
| Astaxanthin |
C₄₀H₅₂O₄ |
596.84 |
Haematococcus pluvialis |
Haematococcus |
Yes |
|
Tetraterpenes |
http://medicinalplants.ynau.edu.cn/meta/bolites/520 |
-- |
| Astramembranoside B |
C₄₁H₇₀O₁₄ |
786.997 |
Astragalus membranaceus |
Leguminosae |
Yes |
|
Triterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC047388 |
Kim JS, Yean MH, Lee EJ, et al. Two new cycloartane saponins from the roots of Astragalus membranaceus. Chem Pharm Bull (Tokyo). 2008;56(1):105-108. doi:10.1248/cpb.56.105 |
| Beesioside P |
C₃₇H₆₂O₁₁ |
682.892 |
Beesia calthifolia |
Ranunculaceae |
Yes |
|
Triterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC047331 |
-- |
| Benzyl 2-Methylbutanoate |
C₁₂H₁₆O₂ |
192.258 |
Artemisia annua |
Asteraceae |
Yes |
|
Hemiterpenes |
http://terokit.qmclab.com/molecule.html?MolId=TKC018727 |
-- |
| Bicusposide E |
C₃₂H₅₂O₇ |
548.761 |
Astragalus bicuspis |
Leguminosae |
No |
|
Triterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC047321 |
Jan S, Abbaskhan A, Musharraf SG, et al. Three new cycloartane triterpenoids from Astragalus bicuspis. Planta Med. 2011;77(16):1829-1834. doi:10.1055/s-0030-1271196 |
| Caldaphnidine F |
C₃₉H₅₅NO₁₃ |
745.863 |
Daphniphyllum calycinum |
Daphniphyllaceae |
Yes |
|
Monoterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC018866 |
Zhan ZJ, Zhang CR, Yue JM. Caldaphnidines A—F, Six New Daphniphyllum Alkaloids from Daphniphyllum calycinum. ChemInform.2006;37.4:11038-11045. doi:10.1002/chin.200604195. |
| Carnosic acid |
C₂₀H₂₈O₄ |
332.43 |
Rosmarinus officinalis |
Labiatae |
Yes |
|
Diterpenoids |
http://medicinalplants.ynau.edu.cn/meta/bolites/539 |
-- |
| Caryopincaolide K |
C₂₀H₂₄O₃ |
312.409 |
Caryopteris incana |
Labiatae |
Yes |
|
Diterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC000004 |
Zhao SM, Chou GX, Yang QS, Wang W, Zhou JL. Abietane diterpenoids from Caryopteris incana (Thunb.) Miq. Org Biomol Chem. 2016;14(14):3510-3520. doi:10.1039/c6ob00139d |
| Cephalotoside A |
C₄₆H₇₈O₁₈ |
919.112 |
Astragalus eremophilus |
Leguminosae |
No |
|
Triterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC047386 |
-- |
| Chagresnone |
C₂₂H₃₄O₄ |
362.51 |
Myrospermum frutescens |
-- |
Yes |
|
Diterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC000032 |
Torres-Mendoza D, Ureña González LD, Ortega-Barría E, et al. Novel cassane and cleistanthane diterpenes from Myrospermum frutescens: absolute stereochemistry of the cassane diterpene series [published correction appears in J Nat Prod. 2006 Aug;69(8):1256]. J Nat Prod. 2004;67(10):1711-1715. doi:10.1021/np049890c |
| Chloranoside A |
C₂₁H₂₈O₉ |
424.446 |
Chloranthus japonicus |
Chloranthaceae |
Yes |
|
Sesquiterpenes |
http://terokit.qmclab.com/molecule.html?MolId=TKC027787 |
Kuang H, Xia Y, Yang B, Wang Q, Lü S. Sesquiterpene Glucosides from Chloranthus japonicus Sieb. Chem Biodivers. 2008;5(9):1736-1742. doi:10.1002/cbdv.200890162 |
| Chlorantene A |
C₁₅H₁₈O₃ |
246.306 |
Chloranthus serratus |
Chloranthaceae |
Yes |
|
Sesquiterpenes |
http://terokit.qmclab.com/molecule.html?MolId=TKC027800 |
Yuan T, Zhang CR, Yang SP, et al. Sesquiterpenoids and phenylpropanoids from Chloranthus serratus. J Nat Prod. 2008;71(12):2021-2025. doi:10.1021/np800543f |
| Cibotiumbaroside A |
C₁₈H₂₀O₁₁ |
412.347 |
Cibotium barometz |
Dicksoniaceae |
Yes |
|
Hemiterpenes |
http://terokit.qmclab.com/molecule.html?MolId=TKC018690 |
Cuong NX, Minh CV, Kiem PV, et al. Inhibitors of osteoclast formation from rhizomes of Cibotium barometz. J Nat Prod. 2009;72(9):1673-1677. doi:10.1021/np9004097 |
| Ciceroside A |
C₅₅H₉₂O₂₃ |
1121.318 |
Astragalus cicer |
Leguminosae |
No |
|
Triterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC047348 |
-- |
| Compound K |
C₃₆H₆₂O₈ |
622.88 |
Panax ginseng |
Araliaceae |
Yes |
|
Triterpenoids |
http://medicinalplants.ynau.edu.cn/meta/bolites/524 |
-- |
| Coronarin H |
C₂₀H₂₈O₃ |
316.441 |
Hedychium coronarium |
Zingiberaceae |
Yes |
|
Diterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC000074 |
-- |
| Curcuminol D |
C₂₀H₃₀O₂ |
302.458 |
Curcuma wenyujin |
Zingiberaceae |
Yes |
|
Diterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC000070 |
Zhang P, Huang W, Song ZH, et al. Min Zhang; Lin Cheng; Yiyu Cheng; Haibin Qu; Zhongjun Ma. Cytotoxic diterpenes from the radix of Curcuma wenyujin. 2008;1(2), 103–106. doi:10.1016/j.phytol.2008.05.001 |
| Cycloartane-3,6,16,20,24,25-Hexol |
C₄₁H₇₀O₁₅ |
802.996 |
Astragalus stereocalyx |
Leguminosae |
No |
|
Triterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC047314 |
Fatih K, Ikhlas AK, Erdal B. Cycloartane-type glycosides from Astragalus schottianus. 2012;5(2),320–324. doi:10.1016/j.phytol.2012.02.011 |
| Cycloartane-3,6,16,24,25-Pentol |
C₄₇H₈₀O₁₉ |
666.893 |
Astragalus boeticus |
Leguminosae |
No |
|
Triterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC047351 |
-- |
| Cycloartane-3,6,16,24,25-Pentol |
C₄₇H₈₀O₁₉ |
949.138 |
Astragalus stereocalyx |
Leguminosae |
No |
|
Triterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC047355 |
-- |
| Cycloascidoside A |
C₄₁H₇₀O₁₄ |
786.997 |
Astragalus eremophilus |
Leguminosae |
No |
|
Triterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC047370 |
-- |
| Cycloasgenin C 3-Xylopyranoside |
C₃₅H₆₀O₉ |
624.856 |
Astragalus eremophilus |
Leguminosae |
No |
|
Triterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC047367 |
-- |
| Cyclobutatusin |
C₂₄H₃₂O₉ |
464.511 |
Plectranthus barbatus |
Labiatae |
Yes |
|
Diterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC000011 |
Raymond Z, David L, Elie CL, et al. Paul. Barbatusin and cyclobutatusin, two novel diterpenoids from coleus barbatus bentham. 1977;33(12),1457–1467. doi:10.1016/0040-4020(77)88005-8 |
| Cyclocanthogenin |
C₃₀H₅₂O₅ |
492.741 |
Astragalus tragacantha |
Leguminosae |
No |
|
Triterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC047373 |
Kim JS, Yean MH, Lee EJ, et al. Two new cycloartane saponins from the roots of Astragalus membranaceus. Chem Pharm Bull (Tokyo). 2008;56(1):105-108. doi:10.1248/cpb.56.105 |
| Cyclocanthoside B |
C₄₃H₇₂O₁₅ |
829.034 |
Astragalus tragacantha |
Leguminosae |
No |
|
Triterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC047376 |
Isaev MI. Iriterpene glycosides of Astragalus and their genins XLIII. Cycloaraloside B from Astragalus amarus. 1992;28(5),461–463. doi:10.1007/bf00630650 |
| Cyclocanthoside G |
C₄₇H₈₀O₁₉ |
949.138 |
Astragalus tragacantha |
Leguminosae |
No |
|
Triterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC047389 |
Isaev MI. Iriterpene glycosides of Astragalus and their genins XLIII. Cycloaraloside B from Astragalus amarus. 1992;28(5),461–463. doi:10.1007/bf00630650 |
| Cyclochivinoside B |
C₄₂H₇₂O₁₅ |
817.023 |
Astragalus chiwensis |
Leguminosae |
No |
|
Triterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC047363 |
-- |
| Cyclochivinoside C |
C₄₂H₇₂O₁₅ |
817.023 |
Astragalus chiwensis |
Leguminosae |
No |
|
Triterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC047382 |
-- |
| Cycloglobiceposide B |
C₄₇H₈₀O₁₉ |
949.138 |
Astragalus eremophilus |
Leguminosae |
No |
|
Triterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC047369 |
Uteniyazov KK, Saatov Z. Levkovich MG, Abdullaev ND. The structure of cycloglobiceposide B fromAstragalus globiceps. 1999;35(2),192–195. doi:10.1007/bf02234933 |
| Cyclomacrogenin B |
C₃₀H₅₂O₅ |
492.741 |
Astragalus macropus |
Leguminosae |
No |
|
Triterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC047333 |
-- |
| Cyclomacroside B |
C₄₅H₇₄O₁₅ |
855.072 |
Astragalus macropus |
Leguminosae |
No |
|
Triterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC047334 |
-- |
| Cyclomacroside C |
C₃₆H₆₂O₉ |
638.883 |
Astragalus macropus |
Leguminosae |
No |
|
Triterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC047336 |
-- |
| Cyclomacroside D |
C₄₁H₇₀O₁₃ |
770.998 |
Astragalus macropus |
Leguminosae |
No |
|
Triterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC047337 |
Labed A, Ferhat M, Labed-Zouad I, et al. Compounds from the pods of Astragalus armatus with antioxidant, anticholinesterase, antibacterial and phagocytic activities. Pharm Biol. 2016;54(12):3026-3032. doi:10.1080/13880209.2016.1200632 |
| Cyclomacroside E |
C₄₆H₇₈O₁₇ |
903.113 |
Astragalus macropus |
Leguminosae |
No |
|
Triterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC047338 |
-- |
| Cyclopside 1 |
C₂₆H₄₀O₁₀ |
512.596 |
Acacia cyclops |
Hemipristidae |
Yes |
|
Monoterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC018855 |
Jelassi A, Zardi-Bergaoui A, Ben Nejma A, Belaiba M, Bouajila J, Ben Jannet H. Two new unusual monoterpene acid glycosides from Acacia cyclops with potential cytotoxic activity. Bioorg Med Chem Lett. 2014;24(16):3777-3781. doi:10.1016/j.bmcl.2014.06.075 |
| Cyclopside 2 |
C₂₆H₄₀O₉ |
496.597 |
Acacia cyclops |
Hemipristidae |
Yes |
|
Monoterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC018856 |
Jelassi A, Zardi-Bergaoui A, Ben Nejma A, Belaiba M, Bouajila J, Ben Jannet H. Two new unusual monoterpene acid glycosides from Acacia cyclops with potential cytotoxic activity. Bioorg Med Chem Lett. 2014;24(16):3777-3781. doi:10.1016/j.bmcl.2014.06.075 |
| Cyclopycnanthoside |
C₄₁H₇₀O₁₄ |
786.997 |
Astragalus eremophilus |
Leguminosae |
No |
|
Triterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC047371 |
-- |
| Cyclostipuloside B |
C₄₆H₇₈O₁₈ |
919.112 |
Astragalus eremophilus |
Leguminosae |
No |
|
Triterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC047368 |
Karimov RZ, Umarova RU, Saatov Z. Levkovich MG, Abdullaev ND. Triterpene glycosides ofTragacanthaand their genins. Cyclostipulosides A and B fromTragacantha stipulosa. 1998;34(5), 609–612. doi:10.1007/bf02319286 |
| Cyclounifolioside A |
C₄₀H₆₆O₁₂ |
738.956 |
Astragalus eremophilus |
Leguminosae |
No |
|
Triterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC047362 |
-- |
| Cyclounifolioside D |
C₃₈H₆₄O₁₁ |
696.919 |
Astragalus eremophilus |
Leguminosae |
No |
|
Triterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC047350 |
-- |
| Daphcalycinosidine A |
C₃₈H₅₁NO₁₂ |
713.821 |
Daphniphyllum calycinum |
Daphniphyllaceae |
Yes |
|
Monoterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC018861 |
Bitar HE , Nguyen VH , Gramain A ,et al. Daphcalycinosidines A and B, new iridoid-alkaloids from Daphniphyllum calycinum[J]. Cheminform. 2004;45(16):515-518. doi:10.1016/j.tetlet.2003.11.005. |
| Daphcalycinosidine B |
C₄₀H₅₇NO₁₃ |
759.89 |
Daphniphyllum calycinum |
Daphniphyllaceae |
Yes |
|
Monoterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC018862 |
Bitar HE , Nguyen VH , Gramain A ,et al. Daphcalycinosidines A and B, new iridoid-alkaloids from Daphniphyllum calycinum[J]. Cheminform. 2004;45(16):515-518. doi:10.1016/j.tetlet.2003.11.005. |
| Daphcalycinosidine C |
C₃₈H₄₉NO₁₂ |
711.805 |
Daphniphyllum calycinum |
Daphniphyllaceae |
Yes |
|
Monoterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC018868 |
El Bitar H, Nguyen VH, Gramain A, Sévenet T, Bodo B. New alkaloids from Daphniphyllum calycinum. J Nat Prod. 2004;67(7):1094-1099. doi:10.1021/np040038f |
| Deacetylasperuloside |
C₁₆H₂₀O₁₀ |
372.326 |
Oldenlandia tenelliflora |
Rubiaceae |
Yes |
|
Monoterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC018871 |
-- |
| Debenzoylpaeoniflorin Aglycone |
C₂₅H₃₂O₁₃ |
630.599 |
Paeonia delavayi |
Paeoniaceae |
Yes |
|
Monoterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC018915 |
-- |
| Debenzoylpaeoniflorin Aglycone |
C₂₅H₃₂O₁₃ |
540.518 |
Paeonia delavayi |
Paeoniaceae |
Yes |
|
Monoterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC018923 |
-- |
| Dendrobane A |
C₁₅H₂₄O₃ |
252.354 |
Dendrobium nobile |
Orchidaceae |
Yes |
|
Sesquiterpenes |
http://terokit.qmclab.com/molecule.html?MolId=TKC027773 |
Ye Q, Zhao W. New alloaromadendrane, cadinene and cyclocopacamphane type sesquiterpene derivatives and bibenzyls from Dendrobium nobile. Planta Med. 2002;68(8):723-729. doi:10.1055/s-2002-33786 |
| Dendronobilin I |
C₁₈H₃₀O₃ |
294.435 |
Dendrobium nobile |
Orchidaceae |
Yes |
|
Sesquiterpenes |
http://terokit.qmclab.com/molecule.html?MolId=TKC027774 |
-- |
| Dendronobilin N |
C₁₅H₂₄O₄ |
268.353 |
Dendrobium nobile |
Orchidaceae |
Yes |
|
Sesquiterpenes |
http://terokit.qmclab.com/molecule.html?MolId=TKC027772 |
Zhang X, Tu FJ, Yu HY, Wang NL, Wang Z, Yao XS. Copacamphane, picrotoxane and cyclocopacamphane sesquiterpenes from Dendrobium nobile. Chem Pharm Bull (Tokyo). 2008;56(6):854-857. doi:10.1248/cpb.56.854 |
| Dendronobiloside E |
C₂₁H₃₄O₈ |
414.495 |
Dendrobium nobile |
Orchidaceae |
Yes |
|
Sesquiterpenes |
http://terokit.qmclab.com/molecule.html?MolId=TKC027775 |
Ye Q, Zhao W. New alloaromadendrane, cadinene and cyclocopacamphane type sesquiterpene derivatives and bibenzyls from Dendrobium nobile. Planta Med. 2002;68(8):723-729. doi:10.1055/s-2002-33786 |
| Desoxysilvaglin |
C₃₀H₄₈O₃ |
456.711 |
Aglaia silvestris |
Meliaceae |
Yes |
|
Triterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC047305 |
-- |
| Dunnianoside J |
C₁₁H₁₈O₈ |
278.257 |
Illicium dunnianum |
Illiciaceae |
Yes |
|
Hemiterpenes |
http://terokit.qmclab.com/molecule.html?MolId=TKC018671 |
Bai J, Chen H, Fang ZF, et al. Sesquiterpenes and neolignans from the roots of Illicium dunnianum. J Asian Nat Prod Res. 2012;14(10):940-949. doi:10.1080/10286020.2012.729507 |
| Ebc 219 |
C₂₀H₂₈O₃ |
316.441 |
Croton insularis |
Euphorbiaceae |
Yes |
|
Diterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC000031 |
Maslovskaya LA, Savchenko AI, Krenske EH, et al. EBC-219: a new diterpene skeleton, crotinsulidane, from the Australian rainforest containing a bridgehead double bond. Angew Chem Int Ed Engl. 2014;53(27):7006-7009. doi:10.1002/anie.201310923 |
| Ebractenoid J |
C₂₀H₂₈O₂ |
300.442 |
Euphorbia ebracteolata |
Euphorbiaceae |
Yes |
|
Diterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC000078 |
Liu ZG, Li ZL, Bai J, et al. Anti-inflammatory diterpenoids from the roots of Euphorbia ebracteolata. J Nat Prod. 2014;77(4):792-799. doi:10.1021/np400873v |
| Eremophiloside A |
C₅₅H₉₂O₂₂ |
1105.319 |
Astragalus eremophilus |
Leguminosae |
No |
|
Triterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC047347 |
-- |
| Eremophiloside B |
C₄₉H₈₂O₁₈ |
959.177 |
Astragalus eremophilus |
Leguminosae |
No |
|
Triterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC047349 |
-- |
| Eremophiloside C |
C₄₁H₇₀O₁₄ |
786.997 |
Astragalus eremophilus |
Leguminosae |
No |
|
Triterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC047323 |
Perrone A, Masullo M, Bassarello C, et al. Unusual cycloartane glycosides from Astragalus eremophilus[J]. Tetrahedron. 2008;64(22):5061-5071. doi:10.1016/j.tet.2008.03.069. |
| Eremophiloside D |
C₄₁H₆₈O₁₄ |
784.981 |
Astragalus eremophilus |
Leguminosae |
No |
|
Triterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC047324 |
Perrone A, Masullo M, Bassarello C, et al. Unusual cycloartane glycosides from Astragalus eremophilus[J]. Tetrahedron. 2008;64(22):5061-5071. doi:10.1016/j.tet.2008.03.069. |
| Euphorbialoid G |
C₃₅H₄₃NO₁₃ |
685.723 |
Euphorbia prolifera |
Euphorbiaceae |
Yes |
|
Diterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC000050 |
Xu J, Jin DQ, Guo Y, et al. New myrsinol diterpenes from Euphorbia prolifera and their inhibitory activities on LPS-induced NO production. Bioorg Med Chem Lett. 2012;22(11):3612-3618. doi:10.1016/j.bmcl.2012.04.052 |
| Euphorbialoid H |
C₄₂H₄₇NO₁₄ |
789.831 |
Euphorbia prolifera |
Euphorbiaceae |
Yes |
|
Diterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC000049 |
Xu J, Jin DQ, Guo Y, et al. New myrsinol diterpenes from Euphorbia prolifera and their inhibitory activities on LPS-induced NO production. Bioorg Med Chem Lett. 2012;22(11):3612-3618. doi:10.1016/j.bmcl.2012.04.052 |
| Euphorbiaproliferin E |
C₄₀H₄₄O₁₃ |
732.779 |
Euphorbia prolifera |
Euphorbiaceae |
Yes |
|
Diterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC000048 |
Xu J, Guo Y, Xie C, et al. Bioactive myrsinol diterpenoids from the roots of Euphorbia prolifera. J Nat Prod. 2011;74(10):2224-2230. doi:10.1021/np200591h |
| Euphorheliosin A |
C₁₃H₂₄O₅ |
260.33 |
Euphorbia helioscopia |
Euphorbiaceae |
Yes |
|
Sesquiterpenes |
http://terokit.qmclab.com/molecule.html?MolId=TKC025341 |
-- |
| Foetidinoside E |
C₄₁H₇₀O₁₅ |
802.996 |
Actaea cimicifuga |
Ranunculaceae |
Yes |
|
Triterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC047332 |
Lu L, Chen JC, Song HJ, Li Y, Nian Y, Qiu MH. Five new triterpene bisglycosides with acyclic side chains from the rhizomes of Cimicifuga foetida L. Chem Pharm Bull (Tokyo). 2010;58(5):729-733. doi:10.1248/cpb.58.729 |
| Foliachinenoside I |
C₁₇H₃₂O₁₁ |
412.432 |
Salacia chinensis |
Celastraceae |
Yes |
|
Hemiterpenes |
http://terokit.qmclab.com/molecule.html?MolId=TKC018738 |
Nakamura S, Zhang Y, Matsuda H, Ninomiya K, Muraoka O, Yoshikawa M. Chemical structures and hepatoprotective effects of constituents from the leaves of Salacia chinensis. Chem Pharm Bull (Tokyo). 2011;59(8):1020-1028. doi:10.1248/cpb.59.1020 |
| Foliasalacioside J |
C₁₉H₃₄O₈ |
390.473 |
Salacia chinensis |
Celastraceae |
Yes |
|
Sesquiterpenes |
http://terokit.qmclab.com/molecule.html?MolId=TKC025418 |
Nakamura S, Zhang Y, Matsuda H, Ninomiya K, Muraoka O, Yoshikawa M. Chemical structures and hepatoprotective effects of constituents from the leaves of Salacia chinensis. Chem Pharm Bull (Tokyo). 2011;59(8):1020-1028. doi:10.1248/cpb.59.1020 |
| Forskoditerpene A |
C₂₀H₃₀O₂ |
302.458 |
Plectranthus barbatus |
Labiatae |
Yes |
|
Diterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC000083 |
Shan Y, Xu L, Lu Y, et al. Diterpenes from Coleus forskohlii (WILLD.) BRIQ. (Labiatae). Chem Pharm Bull (Tokyo). 2008;56(1):52-56. doi:10.1248/cpb.56.52 |
| Friedelin |
C₃₀H₅₀O |
426.72 |
Tripterygium wilfordii |
Celastraceae |
Yes |
|
Triterpenoids |
http://medicinalplants.ynau.edu.cn/meta/bolites/573 |
-- |
| Fukinospirolide A |
C₁₅H₂₀O₄ |
264.321 |
Ligularia virgaurea |
Asteraceae |
Yes |
|
Sesquiterpenes |
http://terokit.qmclab.com/molecule.html?MolId=TKC027756 |
Saito Y, Takashima Y, Kamada A, et al. Chemical and genetic diversity of Ligularia virgaurea collected in northern Sichuan and adjacent areas of China. Isolation of 13 new compound[J]. Tetrahedron. 2012. doi:10.1016/j.tet.2012.09.042. |
| Fukinospirolide B |
C₁₇H₂₂O₅ |
306.358 |
Ligularia virgaurea |
Asteraceae |
Yes |
|
Sesquiterpenes |
http://terokit.qmclab.com/molecule.html?MolId=TKC027757 |
Saito Y, Takashima Y, Kamada A, et al. Chemical and genetic diversity of Ligularia virgaurea collected in northern Sichuan and adjacent areas of China. Isolation of 13 new compound[J]. Tetrahedron. 2012. doi:10.1016/j.tet.2012.09.042. |
| Ginsenoside Rg3 |
C₄₂H₇₂O₁₃ |
785.01 |
Panax ginseng |
Araliaceae |
Yes |
|
Triterpenoids |
http://medicinalplants.ynau.edu.cn/meta/bolites/541 |
-- |
| Ginsenoside Rh2 |
C₃₆H₆₂O₈ |
622.87 |
Panax ginseng |
Araliaceae |
Yes |
|
Triterpenoids |
http://medicinalplants.ynau.edu.cn/meta/bolites/540 |
-- |
| Glycyrrhetinic acid |
C₃₀H₄₆O₄ |
470.69 |
Glycyrrhize glabra |
Leguminosae |
Yes |
|
Diterpenoids |
http://medicinalplants.ynau.edu.cn/meta/bolites/542 |
-- |
| Herbalbin |
C₁₅H₂₂O₄ |
266.337 |
Artemisia herba-alba |
Asteraceae |
Yes |
|
Sesquiterpenes |
http://terokit.qmclab.com/molecule.html?MolId=TKC00754510.1515/znc-2013-9-1001 |
Mohamed Ael-H, Esmail AM, El-Saade AM. Terpenes from Artemisia herba-alba. Z Naturforsch C J Biosci. 2013;68(9-10):343-346. doi:10.1515/znc-2013-9-1001 |
| Huangqiyenin B |
C₃₆H₆₀O₁₀ |
652.866 |
Astragalus membranaceus |
Leguminosae |
Yes |
|
Triterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC047392 |
Wang T, Ruan J, Li X, et al. Bioactive cyclolanstane-type saponins from the stems of Astragalus membranaceus (Fisch.) Bge. var. mongholicus (Bge.) Hsiao. J Nat Med. 2016;70(2):198-206. doi:10.1007/s11418-015-0959-8 |
| Hymenoside A |
C₂₇H₃₂O₁₁ |
532.542 |
Hymenophyllum barbatum |
Hymenophyllaceae |
Yes |
|
Hemiterpenes |
http://terokit.qmclab.com/molecule.html?MolId=TKC018750 |
Oiso Y, Toyota M, Asakawa Y. Hymenosides A-F, six new hemiterpene glucosides from the Japanese fern Hymenophyllum barbatum. Chem Pharm Bull (Tokyo). 2001;49(1):126-128. doi:10.1248/cpb.49.126 |
| Hymenoside B |
C₂₇H₃₂O₁₃ |
564.54 |
Hymenophyllum barbatum |
Hymenophyllaceae |
Yes |
|
Hemiterpenes |
http://terokit.qmclab.com/molecule.html?MolId=TKC018747 |
Oiso Y, Toyota M, Asakawa Y. Hymenosides A-F, six new hemiterpene glucosides from the Japanese fern Hymenophyllum barbatum. Chem Pharm Bull (Tokyo). 2001;49(1):126-128. doi:10.1248/cpb.49.126 |
| Hymenoside E |
C₂₇H₃₂O₁₃ |
564.54 |
Hymenophyllum barbatum |
Hymenophyllaceae |
Yes |
|
Hemiterpenes |
http://terokit.qmclab.com/molecule.html?MolId=TKC018748 |
Oiso Y, Toyota M, Asakawa Y. Hymenosides A-F, six new hemiterpene glucosides from the Japanese fern Hymenophyllum barbatum. Chem Pharm Bull (Tokyo). 2001;49(1):126-128. doi:10.1248/cpb.49.126 |
| Hymenoside F |
C₃₅H₃₈O₁₅ |
698.674 |
Hymenophyllum barbatum |
Hymenophyllaceae |
Yes |
|
Hemiterpenes |
http://terokit.qmclab.com/molecule.html?MolId=TKC018749 |
Oiso Y, Toyota M, Asakawa Y. Hymenosides A-F, six new hemiterpene glucosides from the Japanese fern Hymenophyllum barbatum. Chem Pharm Bull (Tokyo). 2001;49(1):126-128. doi:10.1248/cpb.49.126 |
| Hymenoside G |
C₃₅H₃₈O₁₇ |
730.672 |
Hymenophyllum barbatum |
Hymenophyllaceae |
Yes |
|
Hemiterpenes |
http://terokit.qmclab.com/molecule.html?MolId=TKC018666 |
-- |
| Hymenoside H |
C₃₅H₃₈O₁₇ |
730.672 |
Hymenophyllum barbatum |
Hymenophyllaceae |
Yes |
|
Hemiterpenes |
http://terokit.qmclab.com/molecule.html?MolId=TKC018667 |
-- |
| Hymenoside L |
C₁₉H₂₆O₁₁ |
430.406 |
Hymenophyllum barbatum |
Hymenophyllaceae |
Yes |
|
Hemiterpenes |
http://terokit.qmclab.com/molecule.html?MolId=TKC018665 |
-- |
| Hymenoside N |
C₂₀H₂₆O₁₁ |
442.417 |
Hymenophyllum barbatum |
Hymenophyllaceae |
Yes |
|
Hemiterpenes |
http://terokit.qmclab.com/molecule.html?MolId=TKC018662 |
-- |
| Isomaltopaeoniflorin |
C₂₉H₃₈O₁₆ |
642.607 |
Paeonia obovata |
Paeoniaceae |
Yes |
|
Monoterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC018891 |
-- |
| Isopentyl Gentiobioside |
C₁₇H₃₂O₁₁ |
412.432 |
Solanum tuberosum |
Solanaceae |
Yes |
|
Hemiterpenes |
http://terokit.qmclab.com/molecule.html?MolId=TKC018742 |
-- |
| Isosilvaglin B |
C₃₀H₄₈O₄ |
472.71 |
Aglaia silvestris |
Meliaceae |
Yes |
|
Triterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC047310 |
-- |
| Krugianoside A |
C₅₂H₈₈O₂₂ |
1065.254 |
Astragalus eremophilus |
Leguminosae |
No |
|
Triterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC047397 |
Denizli N, Horo I, Gülcemal D, et al. Cycloartane glycosides from Astragalus plumosus var. krugianus and evaluation of their antioxidant potential. Fitoterapia. 2014;92:211-218. doi:10.1016/j.fitote.2013.10.018 |
| Limonene |
C₁₀H₁₆ |
136.23 |
Solanum lycopersicum |
Solanaceae |
Yes |
|
Monoterpenoids |
http://medicinalplants.ynau.edu.cn/meta/bolites/528 |
-- |
| Linderanlide F |
C₁₇H₂₀O₅ |
304.342 |
Lindera aggregata |
Lauraceae |
Yes |
|
Sesquiterpenes |
http://terokit.qmclab.com/molecule.html?MolId=TKC027788 |
Qiang Y, Yang ZD, Yang JL, Gao K. Sesquiterpenoids from the root tubers of Lindera aggregata. Planta Med. 2011;77(14):1610-1616. doi:10.1055/s-0030-1270922 |
| Linderolide K |
C₁₅H₂₀O₄ |
264.321 |
Lindera aggregata |
Lauraceae |
Yes |
|
Sesquiterpenes |
http://terokit.qmclab.com/molecule.html?MolId=TKC027789 |
Liu Q, Ahn JH, Kim SB, Lee C, Hwang BY, Lee MK. Sesquiterpene lactones from the roots of Lindera strychnifolia. Phytochemistry. 2013;87:112-118. doi:10.1016/j.phytochem.2012.11.004 |
| Linderolide P |
C₁₅H₂₀O₄ |
264.321 |
Lindera aggregata |
Lauraceae |
Yes |
|
Sesquiterpenes |
http://terokit.qmclab.com/molecule.html?MolId=TKC027790 |
Liu Q, Jo YH, Kim SB, Jin Q, Hwang BY, Lee MK. Sesquiterpenes from the roots of Lindera strychnifolia with inhibitory effects on nitric oxide production in RAW 264.7 cells. Bioorg Med Chem Lett. 2016;26(20):4950-4954. doi:10.1016/j.bmcl.2016.09.012 |
| Lycopene |
C₄₀H₅₆ |
536.88 |
Solanum lycopersicum |
Solanaceae |
Yes |
|
Tetraterpenes |
http://medicinalplants.ynau.edu.cn/meta/bolites/521 |
-- |
| Macrophyllosaponin A |
C₄₃H₇₂O₁₄ |
813.035 |
Astragalus oleifolius |
Leguminosae |
Yes |
|
Triterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC047341 |
-- |
| Macrophyllosaponin B |
C₄₁H₇₀O₁₃ |
770.998 |
Astragalus oleifolius |
Leguminosae |
Yes |
|
Triterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC047343 |
-- |
| Macrophyllosaponin C |
C₄₂H₇₂O₁₄ |
801.024 |
Astragalus oleifolius |
Leguminosae |
Yes |
|
Triterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC047342 |
-- |
| Macrophyllosaponin D |
C₄₆H₇₈O₁₇ |
903.113 |
Astragalus oleifolius |
Leguminosae |
Yes |
|
Triterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC047344 |
-- |
| Macrophyllosaponin E |
C₄₂H₇₂O₁₅ |
817.023 |
Astragalus oleifolius |
Leguminosae |
Yes |
|
Triterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC047340 |
Bedir E, Calis I, Khan IA. Macrophyllosaponin E: a novel compound from the roots of Astragalus. oleifolius. Chem Pharm Bull (Tokyo). 2000;48(7):1081-1083. doi:10.1248/cpb.48.1081 |
| Miltiradiene |
C₂₀H₃₂ |
272.47 |
Salvia miltiorrhiza |
Labiatae |
Yes |
|
Diterpenoids |
http://medicinalplants.ynau.edu.cn/meta/bolites/537 |
-- |
| Mioganal |
C₂₀H₂₈O₂ |
300.442 |
Zingiber mioga |
Zingiberaceae |
Yes |
|
Diterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC000082 |
-- |
| Mongholicoside B |
C₃₆H₆₀O₁₁ |
668.865 |
Astragalus mongholicus |
Leguminosae |
No |
|
Triterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC047313 |
Yu QT, Li P, Bi ZM, et al. Two new saponins from the aerial part of Astragalus membranaceus var. mongholicus[J]. Chinese Chemical Letters. 2007(005):018. doi:10.1016/j.cclet.2007.03.025. |
| Nardosinanone A |
C₁₅H₂₄O₃ |
252.354 |
Nardostachys jatamansi |
Valerianaceae |
Yes |
|
Sesquiterpenes |
http://terokit.qmclab.com/molecule.html?MolId=TKC027792 |
Zhang JB, Liu ML, Duan YH, et al. Novel nardosinane type sesquiterpenoids from Nardostachys chinensis Batal[J]. Tetrahedron. 2014(70-30). doi:10.1016/j.tet.2014.05.010. |
| Nervonin A |
C₂₈H₃₈O₁₀ |
534.602 |
Isodon nervosus |
Labiatae |
Yes |
|
Diterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC000081 |
Li LM, Li GY, Ding LS, et al. ent-Kaurane Diterpenoids from Isodon nervosus. J Nat Prod. 2008;71(4):684-688. doi:10.1021/np800027a |
| Nonioside N |
C₁₇H₃₀O₁₂ |
426.415 |
Morinda citrifolia |
Rubiaceae |
Yes |
|
Hemiterpenes |
http://terokit.qmclab.com/molecule.html?MolId=TKC018728 |
Akihisa T, Seino K, Kaneko E, et al. Melanogenesis inhibitory activities of iridoid-, hemiterpene-, and fatty acid-glycosides from the fruits of Morinda citrifolia (Noni). J Oleo Sci. 2010;59(1):49-57. doi:10.5650/jos.59.49 |
| Nonioside O |
C₁₆H₂₈O₁₁ |
396.389 |
Morinda citrifolia |
Rubiaceae |
Yes |
|
Hemiterpenes |
http://terokit.qmclab.com/molecule.html?MolId=TKC018730 |
Akihisa T, Seino K, Kaneko E, et al. Melanogenesis inhibitory activities of iridoid-, hemiterpene-, and fatty acid-glycosides from the fruits of Morinda citrifolia (Noni). J Oleo Sci. 2010;59(1):49-57. doi:10.5650/jos.59.49 |
| Nootkatone |
C₁₅H₂₂O |
218.34 |
Citrus paradisi |
Rutaceae |
Yes |
|
Sesquiterpenes |
http://medicinalplants.ynau.edu.cn/meta/bolites/517 |
-- |
| Notoginsenoside R1 |
C₄₇H₈₀O₁₈ |
933.13 |
Panax notoginseng |
Araliaceae |
Yes |
|
Triterpenoids |
http://medicinalplants.ynau.edu.cn/meta/bolites/518 |
-- |
| Oleanolic Acid |
C₃₀H₄₈O₃ |
456.711 |
Viscum coloratum |
Loranthaceae |
Yes |
|
Triterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC022686 |
Gallo MB, Marques AS, Vieira PC, et al. Enzymatic inhibitory activity and trypanocidal effects of extracts and compounds from Siphoneugena densiflora O. Berg and Vitex polygama Cham. Z Naturforsch C J Biosci. 2008;63(5-6):371-382. doi:10.1515/znc-2008-5-611 |
| Oleanolic acid |
C₃₀H₄₈O₃ |
456.7 |
Ligustrum lucidum |
Oleaceae |
Yes |
|
Triterpenoids |
http://medicinalplants.ynau.edu.cn/meta/bolites/527 |
-- |
| Osmaronin |
C₁₁H₁₇NO₆ |
259.258 |
Prinsepia utilis |
Rosaceae |
Yes |
|
Hemiterpenes |
http://terokit.qmclab.com/molecule.html?MolId=TKC018678 |
Cyanoglucosides in the epidermis of Hordeum vulgare[J]. Phytochemistry. 1993;33(2):295-297. doi:10.1016/0031-9422(93)85506-M. |
| Patchoulol |
C₁₅H₂₆O |
222.37 |
Pogostemon cablin |
Labiatae |
Yes |
|
Sesquiterpenes |
http://medicinalplants.ynau.edu.cn/meta/bolites/535 |
-- |
| Platanionoside B |
C₂₅H₄₂O₁₂ |
534.599 |
Alangium platanifolium |
Cornaceae |
Yes |
|
Sesquiterpenes |
http://terokit.qmclab.com/molecule.html?MolId=TKC025186 |
Tamaki A, Otsuka H, Ide T. Platanionosides A-C, megastigmane diglycosides from the leaves of Alangium platanifolium. J Nat Prod. 1999;62(7):1074-1076. doi:10.1021/np990050l |
| Plectrornatin A |
C₂₃H₃₄O₅ |
390.52 |
Plectranthus ornatus |
Labiatae |
Yes |
|
Sesquiterpenes |
http://terokit.qmclab.com/molecule.html?MolId=TKC008999 |
Rijo P, Gaspar-Marques C, Simões MF, et al. Neoclerodane and labdane diterpenoids from Plectranthus ornatus. J Nat Prod. 2002;65(10):1387-1390. doi:10.1021/np020203w |
| Prinsepicyanoside B |
C₁₅H₂₁NO₇ |
327.333 |
Prinsepia utilis |
Rosaceae |
Yes |
|
Hemiterpenes |
http://terokit.qmclab.com/molecule.html?MolId=TKC018673 |
Guan B, Li T, Xu XK, et al. γ-Hydroxynitrile glucosides from the seeds of Prinsepia utilis. Phytochemistry. 2014;105:135-140. doi:10.1016/j.phytochem.2014.05.018 |
| Prinsepicyanoside D |
C₁₅H₂₁NO₈ |
343.332 |
Prinsepia utilis |
Rosaceae |
Yes |
|
Hemiterpenes |
http://terokit.qmclab.com/molecule.html?MolId=TKC018636 |
Guan B, Li T, Xu XK, et al. γ-Hydroxynitrile glucosides from the seeds of Prinsepia utilis. Phytochemistry. 2014;105:135-140. doi:10.1016/j.phytochem.2014.05.018 |
| Prinsepicyanoside E |
C₁₇H₂₇NO₈ |
373.402 |
Prinsepia utilis |
Rosaceae |
Yes |
|
Hemiterpenes |
http://terokit.qmclab.com/molecule.html?MolId=TKC018677 |
Guan B, Li T, Xu XK, et al. γ-Hydroxynitrile glucosides from the seeds of Prinsepia utilis. Phytochemistry. 2014;105:135-140. doi:10.1016/j.phytochem.2014.05.018 |
| Protopanaxadiol |
C₃₀H₅₂O₃ |
460.73 |
Panax ginseng |
Araliaceae |
Yes |
|
Triterpenoids |
http://medicinalplants.ynau.edu.cn/meta/bolites/519 |
-- |
| Rehmaglutoside A |
C₂₄H₃₀O₁₀ |
478.494 |
Rehmannia glutinosa |
Orobanchaceae |
Yes |
|
Monoterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC018945 |
Liu YF, Liang D, Luo H, et al. Hepatoprotective iridoid glycosides from the roots of Rehmannia glutinosa. J Nat Prod. 2012;75(9):1625-1631. doi:10.1021/np300509z |
| Rehmaglutoside B |
C₂₉H₄₀O₁₇ |
660.622 |
Rehmannia glutinosa |
Orobanchaceae |
Yes |
|
Monoterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC018955 |
Liu YF, Liang D, Luo H, et al. Hepatoprotective iridoid glycosides from the roots of Rehmannia glutinosa. J Nat Prod. 2012;75(9):1625-1631. doi:10.1021/np300509z |
| Rehmaglutoside C |
C₃₀H₄₂O₁₇ |
674.649 |
Rehmannia glutinosa |
Orobanchaceae |
Yes |
|
Monoterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC018952 |
Liu YF, Liang D, Luo H, et al. Hepatoprotective iridoid glycosides from the roots of Rehmannia glutinosa. J Nat Prod. 2012;75(9):1625-1631. doi:10.1021/np300509z |
| Rehmaglutoside D |
C₂₃H₃₁NO₁₁ |
497.497 |
Rehmannia glutinosa |
Orobanchaceae |
Yes |
|
Monoterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC018961 |
Liu YF, Liang D, Luo H, et al. Hepatoprotective iridoid glycosides from the roots of Rehmannia glutinosa. J Nat Prod. 2012;75(9):1625-1631. doi:10.1021/np300509z |
| Rehmannioside C |
C₂₁H₃₄O₁₄ |
510.489 |
Rehmannia glutinosa |
Orobanchaceae |
Yes |
|
Monoterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC018954 |
-- |
| Retusolide A |
C₂₀H₂₆O₄ |
330.424 |
Euphorbia retusa |
Euphorbiaceae |
Yes |
|
Diterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC000073 |
-- |
| Retusolide C |
C₂₀H₂₄O₃ |
312.409 |
Euphorbia retusa |
Euphorbiaceae |
Yes |
|
Diterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC000098 |
Haba H, Lavaud C, Magid AA, Benkhaled M. Diterpenoids and triterpenoids from Euphorbia retusa. J Nat Prod. 2009;72(7):1258-1264. doi:10.1021/np900127j |
| Retusolide D |
C₂₀H₂₄O₄ |
328.408 |
Euphorbia retusa |
Euphorbiaceae |
Yes |
|
Diterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC000072 |
Haba H, Lavaud C, Magid AA, Benkhaled M. Diterpenoids and triterpenoids from Euphorbia retusa. J Nat Prod. 2009;72(7):1258-1264. doi:10.1021/np900127j |
| Rhobupcyanoside A |
C₂₀H₂₅NO₁₁ |
455.416 |
Rhodiola bupleuroides |
Crassulaceae |
Yes |
|
Hemiterpenes |
http://terokit.qmclab.com/molecule.html?MolId=TKC018630 |
Chai YQ, Zhao GH, Wang RJ, Cao MG, Wu HB, et al. Hong-quan Duan. Anti-tumor metastatic constituents from Ｒhodiola wallichiana. China Journal of Chinese Materia Medica. 2015;40(2):258-63. doi:10.4268/cjcmm20150218 |
| Rhodiocyanoside B |
C₁₈H₂₁NO₁₁ |
427.362 |
Rhodiola quadrifida |
Crassulaceae |
Yes |
|
Hemiterpenes |
http://terokit.qmclab.com/molecule.html?MolId=TKC018634 |
Yoshikawa M, Shimada H, Shimoda H, Matsuda H, Yamahara J, Murakami N. Rhodiocyanosides A and B, new antiallergic cyanoglycosides from Chinese natural medicine "si lie hong jing tian", the underground part of Rhodiola quadrifida (Pall.) Fisch. et Mey. Chem Pharm Bull (Tokyo). 1995;43(7):1245-1247. doi:10.1248/cpb.43.1245 |
| Rhodiocyanoside D |
C₁₁H₁₇NO₆ |
259.258 |
Rhodiola sacra |
Crassulaceae |
Yes |
|
Hemiterpenes |
http://terokit.qmclab.com/molecule.html?MolId=TKC018669 |
Yoshikawa M, Shimada H, Horikawa S, et al. Bioactive constituents of Chinese natural medicines. IV. Rhodiolae radix. (2).: On the histamine release inhibitors from the underground part of Rhodiola sacra (Prain ex Hamet) S. H. Fu (Crassulaceae): chemical structures of rhodiocyanoside D and sacranosides A and B. Chem Pharm Bull (Tokyo). 1997;45(9):1498-1503. doi:10.1248/cpb.45.1498 |
| Sabinene |
C₁₀H₁₆ |
136.23 |
Solanum lycopersicum |
Solanaceae |
Yes |
|
Diterpenoids |
http://medicinalplants.ynau.edu.cn/meta/bolites/529 |
-- |
| Salicifoline |
C₃₆H₅₀O₁₇ |
754.779 |
Euphorbia salicifolia |
Euphorbiaceae |
Yes |
|
Diterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC000053 |
-- |
| Saprorthoquinone |
C₂₀H₂₄O₂ |
296.41 |
Salvia prionitis |
Labiatae |
Yes |
|
Diterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC000066 |
Simões F, Michavila A, Rodríguez B, Maria C, Alvarez G, Hasan M. A quinone methide diterpenoid from the root of Salvia moorciuftiana. 1986;25(3),755–756. doi:10.1016/0031-9422(86)88043-8 |
| Sarcaglaboside F |
C₂₁H₂₈O₁₀ |
440.445 |
Sarcandra glabra |
Chloranthaceae |
Yes |
|
Sesquiterpenes |
http://terokit.qmclab.com/molecule.html?MolId=TKC027786 |
Hu XR, Yang JS, Xu XD. Three novel sesquiterpene glycosides of Sarcandra glabra. Chem Pharm Bull (Tokyo). 2009;57(4):418-420. doi:10.1248/cpb.57.418 |
| Sclareol |
C₂₀H₃₆O₂ |
308.51 |
Salvia sclarea |
Labiatae |
Yes |
|
Diterpenoids |
http://medicinalplants.ynau.edu.cn/meta/bolites/536 |
-- |
| Sesquilimonene |
C₁₅H₂₄ |
204.357 |
Curcuma longa |
Zingiberaceae |
Yes |
|
Sesquiterpenes |
http://terokit.qmclab.com/molecule.html?MolId=TKC018836 |
-- |
| Shizukanolide E |
C₁₅H₁₈O₄ |
262.305 |
Chloranthus serratus |
Chloranthaceae |
Yes |
|
Sesquiterpenes |
http://terokit.qmclab.com/molecule.html?MolId=TKC027785 |
-- |
| Staphylionoside E |
C₁₉H₃₂O₈ |
388.457 |
Staphylea bumalda |
Vitaceae |
Yes |
|
Sesquiterpenes |
http://terokit.qmclab.com/molecule.html?MolId=TKC025215 |
Yu Q, Matsunami K, Otsuka H, Takeda Y. Staphylionosides A-K: megastigmane glucosides from the leaves of Staphylea bumalda DC. Chem Pharm Bull (Tokyo). 2005;53(7):800-807. doi:10.1248/cpb.53.800
|
| Staphylionoside G |
C₂₅H₄₂O₁₂ |
534.599 |
Staphylea bumalda |
Vitaceae |
Yes |
|
Sesquiterpenes |
http://terokit.qmclab.com/molecule.html?MolId=TKC025187 |
Yu Q, Matsunami K, Otsuka H, Takeda Y. Staphylionosides A-K: megastigmane glucosides from the leaves of Staphylea bumalda DC. Chem Pharm Bull (Tokyo). 2005;53(7):800-807. doi:10.1248/cpb.53.800 |
| Sutherlandioside B |
C₃₆H₆₀O₁₀ |
652.866 |
Lessertia frutescens |
Leguminosae |
Yes |
|
Triterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC047345 |
Fu X, Li XC, Smillie TJ, et al. Cycloartane glycosides from Sutherlandia frutescens. J Nat Prod. 2008;71(10):1749-1753. doi:10.1021/np800328r |
| Taraxien |
C₇₂H₁₁₆O₅ |
1061.715 |
Taraxacum officinale |
Asteraceae |
Yes |
|
Tetraterpenes |
http://terokit.qmclab.com/molecule.html?MolId=TKC046786 |
-- |
| Taxadiene |
C₂₀H₃₂ |
272.49 |
Taxus chinensis |
Taxaceae |
Yes |
|
Diterpenoids |
http://medicinalplants.ynau.edu.cn/meta/bolites/572 |
-- |
| Teneoside A |
C₂₂H₃₀O₁₄ |
518.468 |
Oldenlandia tenelliflora |
Rubiaceae |
Yes |
|
Monoterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC018880 |
-- |
| Torilenol |
C₁₅H₂₄O |
220.356 |
Torilis japonica |
Umbelliferae |
Yes |
|
Sesquiterpenes |
http://terokit.qmclab.com/molecule.html?MolId=TKC027808 |
Liu LL, Ha TK, Ha W, Oh WK, Yang JL, Shi YP. Sesquiterpenoids with Various Carbocyclic Skeletons from the Flowers of Chrysanthemum indicum. J Nat Prod. 2017;80(2):298-307. doi:10.1021/acs.jnatprod.6b00694 |
| Trojanoside E |
C₅₃H₉₀O₂₃ |
1095.28 |
Astragalus eremophilus |
Leguminosae |
No |
|
Triterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC047400 |
-- |
| Trojanoside F |
C₅₂H₈₈O₂₃ |
1081.253 |
Astragalus eremophilus |
Leguminosae |
No |
|
Triterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC047380 |
-- |
| Turpinionoside D |
C₁₉H₃₄O₈ |
390.473 |
Turpinia ternata |
Staphyleaceae |
Yes |
|
Sesquiterpenes |
http://terokit.qmclab.com/molecule.html?MolId=TKC025381 |
Yu Q, Otsuka H, Hirata E, Shinzato T, Takeda Y. Turpinionosides A-E: megastigmane glucosides from leaves of Turpinia ternata Nakai. Chem Pharm Bull (Tokyo). 2002;50(5):640-644. doi:10.1248/cpb.50.640 |
| Usitatissimin A |
C₂₀H₂₈O₃ |
316.441 |
Linum usitatissimum |
Linaceae |
Yes |
|
Diterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC000052 |
Sun JL, Deng AJ, Li Y, Li ZH, Chen H, Qin HL. First Example of Diterpenoids from 14,15-Cyclopimarane in the Roots of Linum usitatissimum. 2009;92(12),2746–2753. doi:10.1002/hlca.200900104 |
| Virgaurenospirolide C |
C₁₅H₁₈O₅ |
278.304 |
Ligularia virgaurea |
Asteraceae |
Yes |
|
Sesquiterpenes |
http://terokit.qmclab.com/molecule.html?MolId=TKC027760 |
Yoshinori, Saito, Saori, et al. Terpenoids from Ligularia virgaurea collected in China: the first example of two bakkane derivatives with an anhydride-type ring C and nineteen new chemical constituents[J]. Tetrahedron. 2015. doi:10.1016/j.tet.2015.09.011. |
| Wallichiiside C |
C₁₇H₂₆O₉ |
374.386 |
Eriophyton wallichii |
Labiatae |
Yes |
|
Monoterpenoids |
http://terokit.qmclab.com/molecule.html?MolId=TKC018948 |
Fan QL, Tan CH, Liu J, Zhao MM, Han FS, Zhu DY. Iridoid glycosides and glycosidic constituents from Eriophyton wallichii Benth. Phytochemistry. 2011;72(14-15):1927-1932. doi:10.1016/j.phytochem.2011.04.019 |
| Wilsonol F |
C₁₃H₂₆O₃ |
230.348 |
Cinnamomum wilsonii |
Lauraceae |
Yes |
|
Sesquiterpenes |
http://terokit.qmclab.com/molecule.html?MolId=TKC025258 |
Shu P, Wei X, Xue Y, et al. Wilsonols A-L, megastigmane sesquiterpenoids from the leaves of Cinnamomum wilsonii. J Nat Prod. 2013;76(7):1303-1312. doi:10.1021/np4002493 |
| Yinxiancaoside A |
C₂₁H₃₀O₉ |
426.462 |
Chloranthus serratus |
Chloranthaceae |
Yes |
|
Sesquiterpenes |
http://terokit.qmclab.com/molecule.html?MolId=TKC027791 |
Kuang H, Xia Y, Yang B, Wang Q, Lü S. Sesquiterpene Glucosides from Chloranthus japonicus Sieb. Chem Biodivers. 2008;5(9):1736-1742. doi:10.1002/cbdv.200890162 |
| α-Terpineol |
C₁₀H₁₈O |
154.25 |
Pinus palustris |
Pinaceae |
No |
|
Monoterpenoids |
http://medicinalplants.ynau.edu.cn/meta/bolites/531 |
-- |
| β-Doradecin |
C₄₀H₅₂O₃ |
580.853 |
Calendula officinalis |
Asteraceae |
Yes |
|
Tetraterpenes |
http://terokit.qmclab.com/molecule.html?MolId=TKC046771 |
-- |